Linked Data
ClinVar Variation Id:
264555
dbSNP Id:
rs756364065
ExAC:
12:2783741 G / A
gnomAD v2:
12-2783741-G-A
gnomAD v3:
12-2674575-G-A
gnomAD v4:
12-2674575-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.2674575G>A , CM000674.2:g.2674575G>A | GRCh38 |
| NC_000012.11:g.2783741G>A , CM000674.1:g.2783741G>A | GRCh37 |
| NC_000012.10:g.2654002G>A | NCBI36 |
| NG_008801.2:g.708790G>A , LRG_334:g.708790G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335762.10:c.4836G>A | ENSP00000336982.5:p.Ala1612= | |
| ENST00000399617.6:c.4761G>A | ENSP00000382526.1:p.Ala1587= | |
| ENST00000399634.6:c.4728G>A | ENSP00000382542.2:p.Ala1576= | |
| ENST00000406454.8:c.4761G>A | ENSP00000385896.3:p.Ala1587= | |
| ENST00000682320.1:n.903G>A | ||
| ENST00000682336.1:c.4803G>A | ENSP00000507898.1:p.Ala1601= | |
| ENST00000682462.1:c.4851G>A | ENSP00000507105.1:p.Ala1617= | |
| ENST00000682544.1:c.4995G>A | ENSP00000507184.1:p.Ala1665= | |
| ENST00000682686.1:c.4728G>A | ENSP00000507309.1:p.Ala1576= | |
| ENST00000682835.1:c.4761G>A | ENSP00000507282.1:p.Ala1587= | |
| ENST00000683482.1:c.4752G>A | ENSP00000507169.1:p.Ala1584= | |
| ENST00000683781.1:c.4851G>A | ENSP00000507434.1:p.Ala1617= | |
| ENST00000683824.1:c.4926G>A | ENSP00000507867.1:p.Ala1642= | |
| ENST00000683840.1:c.4851G>A | ENSP00000507612.1:p.Ala1617= | |
| ENST00000683956.1:c.4851G>A | ENSP00000506882.1:p.Ala1617= | |
| ENST00000684467.1:n.1264G>A | ||
| ENST00000327702.12:c.4761G>A | ENSP00000329877.7:p.Ala1587= | |
| ENST00000347598.9:c.4905G>A | ENSP00000266376.6:p.Ala1635= | |
| ENST00000399603.6:c.4761G>A MANE Plus Clinical | ENSP00000382512.1:p.Ala1587= | |
| ENST00000399641.6:c.4761G>A | ENSP00000382549.1:p.Ala1587= | |
| ENST00000399655.6:c.4761G>A MANE Select | ENSP00000382563.1:p.Ala1587= | |
| ENST00000327702.11:c.4761G>A | ENSP00000329877.7:p.Ala1587= | |
| ENST00000335762.9:c.4836G>A | ENSP00000336982.5:p.Ala1612= | |
| ENST00000344100.7:c.4884G>A | ENSP00000341092.3:p.Ala1628= | |
| ENST00000347598.8:c.4905G>A | ENSP00000266376.6:p.Ala1635= | |
| ENST00000399591.5:c.4785G>A | ENSP00000382500.1:p.Ala1595= | |
| ENST00000399595.5:c.4785G>A | ENSP00000382504.1:p.Ala1595= | |
| ENST00000399597.5:c.4761G>A | ENSP00000382506.1:p.Ala1587= | |
| ENST00000399601.5:c.4761G>A | ENSP00000382510.1:p.Ala1587= | |
| ENST00000399603.5:c.4761G>A | ENSP00000382512.1:p.Ala1587= | |
| ENST00000399606.5:c.4821G>A | ENSP00000382515.1:p.Ala1607= | |
| ENST00000399617.5:c.4761G>A | ENSP00000382526.1:p.Ala1587= | |
| ENST00000399621.5:c.4818G>A | ENSP00000382530.1:p.Ala1606= | |
| ENST00000399629.5:c.4812G>A | ENSP00000382537.1:p.Ala1604= | |
| ENST00000399634.5:c.4761G>A | ENSP00000382542.1:p.Ala1587= | |
| ENST00000399637.5:c.4818G>A | ENSP00000382546.1:p.Ala1606= | |
| ENST00000399638.5:c.4845G>A | ENSP00000382547.1:p.Ala1615= | |
| ENST00000399641.5:c.4761G>A | ENSP00000382549.1:p.Ala1587= | |
| ENST00000399644.5:c.4761G>A | ENSP00000382552.1:p.Ala1587= | |
| ENST00000399649.5:c.4779G>A | ENSP00000382557.1:p.Ala1593= | |
| ENST00000399655.5:c.4761G>A | ENSP00000382563.1:p.Ala1587= | |
| ENST00000402845.7:c.4818G>A | ENSP00000385724.3:p.Ala1606= | |
| ENST00000406454.7:c.4761G>A | ENSP00000385896.3:p.Ala1587= | |
| ENST00000465934.1:n.305G>A | ||
| ENST00000613940.4:c.4284G>A | ENSP00000483335.1:p.Ala1428= | |
| ENST00000615303.4:c.4428G>A | ENSP00000480922.1:p.Ala1476= | |
| ENST00000615400.4:c.4428G>A | ENSP00000480292.1:p.Ala1476= | |
| ENST00000616390.1:c.834G>A | ENSP00000482910.1:p.Ala278= | |
| ENST00000620878.4:c.4251G>A | ENSP00000479029.1:p.Ala1417= | |
| ENST00000621625.4:c.4284G>A | ENSP00000484796.1:p.Ala1428= | |
| NM_000719.6:c.4761G>A , LRG_334t1:c.4761G>A | NP_000710.5:p.Ala1587= | |
| NM_001129827.1:c.4905G>A , LRG_334t2:c.4905G>A | NP_001123299.1:p.Ala1635= | |
| NM_001129829.1:c.4884G>A | NP_001123301.1:p.Ala1628= | |
| NM_001129830.2:c.4761G>A | NP_001123302.2:p.Ala1587= | |
| NM_001129831.1:c.4845G>A | NP_001123303.1:p.Ala1615= | |
| NM_001129832.1:c.4821G>A | NP_001123304.1:p.Ala1607= | |
| NM_001129833.1:c.4818G>A | NP_001123305.1:p.Ala1606= | |
| NM_001129834.1:c.4818G>A | NP_001123306.1:p.Ala1606= | |
| NM_001129835.1:c.4818G>A | NP_001123307.1:p.Ala1606= | |
| NM_001129836.1:c.4812G>A | NP_001123308.1:p.Ala1604= | |
| NM_001129837.1:c.4785G>A | NP_001123309.1:p.Ala1595= | |
| NM_001129838.1:c.4785G>A | NP_001123310.1:p.Ala1595= | |
| NM_001129839.1:c.4779G>A | NP_001123311.1:p.Ala1593= | |
| NM_001129840.1:c.4761G>A , LRG_334t4:c.4761G>A | NP_001123312.1:p.Ala1587= | |
| NM_001129841.1:c.4761G>A | NP_001123313.1:p.Ala1587= | |
| NM_001129842.1:c.4761G>A | NP_001123314.1:p.Ala1587= | |
| NM_001129843.1:c.4761G>A | NP_001123315.1:p.Ala1587= | |
| NM_001129844.1:c.4752G>A | NP_001123316.1:p.Ala1584= | |
| NM_001129846.1:c.4728G>A | NP_001123318.1:p.Ala1576= | |
| NM_001167623.1:c.4761G>A | NP_001161095.1:p.Ala1587= | |
| NM_001167624.2:c.4761G>A | NP_001161096.2:p.Ala1587= | |
| NM_001167625.1:c.4728G>A | NP_001161097.1:p.Ala1576= | |
| NM_199460.3:c.4905G>A | NP_955630.3:p.Ala1635= | |
| XM_006719017.1:c.4851G>A | XP_006719080.1:p.Ala1617= | |
| XM_011521017.1:c.4062G>A | XP_011519319.1:p.Ala1354= | |
| XM_011521018.1:c.3507G>A | XP_011519320.1:p.Ala1169= | |
| XM_011521019.1:c.1617G>A | XP_011519321.1:p.Ala539= | |
| XM_011521020.1:c.4926G>A | XP_011519322.1:p.Ala1642= | |
| XM_011521021.1:c.4761G>A | XP_011519323.1:p.Ala1587= | |
| XM_011521022.1:c.4761G>A | XP_011519324.1:p.Ala1587= | |
| XM_011521023.1:c.4836G>A | XP_011519325.1:p.Ala1612= | |
| XM_006719017.2:c.4851G>A | XP_006719080.1:p.Ala1617= | |
| XM_011521020.2:c.4926G>A | XP_011519322.1:p.Ala1642= | |
| XM_011521023.3:c.4836G>A | XP_011519325.1:p.Ala1612= | |
| XM_017019926.2:c.5265G>A | XP_016875415.1:p.Ala1755= | |
| XM_017019927.2:c.5265G>A | XP_016875416.1:p.Ala1755= | |
| XM_017019928.2:c.5265G>A | XP_016875417.1:p.Ala1755= | |
| XM_017019929.2:c.5208G>A | XP_016875418.1:p.Ala1736= | |
| XM_017019930.2:c.5208G>A | XP_016875419.1:p.Ala1736= | |
| XM_017019931.2:c.5124G>A | XP_016875420.1:p.Ala1708= | |
| XM_017019932.2:c.4896G>A | XP_016875421.1:p.Ala1632= | |
| XM_017019933.2:c.5013G>A | XP_016875422.1:p.Ala1671= | |
| XM_017019934.2:c.5004G>A | XP_016875423.1:p.Ala1668= | |
| XM_017019935.2:c.5004G>A | XP_016875424.1:p.Ala1668= | |
| XM_017019936.2:c.4986G>A | XP_016875425.1:p.Ala1662= | |
| XM_017019937.2:c.4986G>A | XP_016875426.1:p.Ala1662= | |
| XM_017019938.2:c.4986G>A | XP_016875427.1:p.Ala1662= | |
| XM_017019939.2:c.4980G>A | XP_016875428.1:p.Ala1660= | |
| XM_017019940.2:c.4953G>A | XP_016875429.1:p.Ala1651= | |
| XM_017019941.2:c.4947G>A | XP_016875430.1:p.Ala1649= | |
| XM_017019942.2:c.4929G>A | XP_016875431.1:p.Ala1643= | |
| XM_017019943.2:c.4929G>A | XP_016875432.1:p.Ala1643= | |
| XM_017019944.2:c.4929G>A | XP_016875433.1:p.Ala1643= | |
| XM_017019945.2:c.4929G>A | XP_016875434.1:p.Ala1643= | |
| XM_017019946.2:c.4929G>A | XP_016875435.1:p.Ala1643= | |
| XM_017019947.2:c.4929G>A | XP_016875436.1:p.Ala1643= | |
| XM_017019948.2:c.4929G>A | XP_016875437.1:p.Ala1643= | |
| XM_017019949.2:c.4929G>A | XP_016875438.1:p.Ala1643= | |
| XM_017019950.2:c.4923G>A | XP_016875439.1:p.Ala1641= | |
| XM_017019951.2:c.4920G>A | XP_016875440.1:p.Ala1640= | |
| XM_017019952.2:c.4896G>A | XP_016875441.1:p.Ala1632= | |
| XM_017019953.1:c.4851G>A | XP_016875442.1:p.Ala1617= | |
| XM_017019954.1:c.4851G>A | XP_016875443.1:p.Ala1617= | |
| XM_017019955.2:c.5004G>A | XP_016875444.1:p.Ala1668= | |
| NM_000719.7:c.4761G>A MANE Select | NP_000710.5:p.Ala1587= | |
| NM_001129827.2:c.4905G>A | NP_001123299.1:p.Ala1635= | |
| NM_001129830.3:c.4761G>A | NP_001123302.2:p.Ala1587= | |
| NM_001129840.2:c.4761G>A | NP_001123312.1:p.Ala1587= | |
| NM_001167623.2:c.4761G>A MANE Plus Clinical | NP_001161095.1:p.Ala1587= | |
| NM_001129829.2:c.4884G>A | NP_001123301.1:p.Ala1628= | |
| NM_001129831.2:c.4845G>A | NP_001123303.1:p.Ala1615= | |
| NM_001129832.2:c.4821G>A | NP_001123304.1:p.Ala1607= | |
| NM_001129833.2:c.4818G>A | NP_001123305.1:p.Ala1606= | |
| NM_001129834.2:c.4818G>A | NP_001123306.1:p.Ala1606= | |
| NM_001129835.2:c.4818G>A | NP_001123307.1:p.Ala1606= | |
| NM_001129836.2:c.4812G>A | NP_001123308.1:p.Ala1604= | |
| NM_001129837.2:c.4785G>A | NP_001123309.1:p.Ala1595= | |
| NM_001129838.2:c.4785G>A | NP_001123310.1:p.Ala1595= | |
| NM_001129839.2:c.4779G>A | NP_001123311.1:p.Ala1593= | |
| NM_001129841.2:c.4761G>A | NP_001123313.1:p.Ala1587= | |
| NM_001129842.2:c.4761G>A | NP_001123314.1:p.Ala1587= | |
| NM_001129843.2:c.4761G>A | NP_001123315.1:p.Ala1587= | |
| NM_001129844.2:c.4752G>A | NP_001123316.1:p.Ala1584= | |
| NM_001129846.2:c.4728G>A | NP_001123318.1:p.Ala1576= | |
| NM_001167624.3:c.4761G>A | NP_001161096.2:p.Ala1587= | |
| NM_001167625.2:c.4728G>A | NP_001161097.1:p.Ala1576= | |
| NM_199460.4:c.4905G>A | NP_955630.3:p.Ala1635= |